| Literature DB >> 592352 |
V Escobar, J Eastman, D Weaver, M Melnick.
Abstract
Four individuals in a single family affected with maxillofacial dysostosis are reported. Maxillary hypoplasia, delayed onset of speech, and poor development of language skills without associated hearing loss are the main characteristics of the syndrome which is transmitted as an autosomal dominant. Cephalometric analysis and speech and hearing evaluation of our patients confirmed the above findings.Entities:
Mesh：
Year: 1977 PMID： 592352 PMCID： PMC1013620 DOI： 10.1136/jmg.14.5.355
Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318